Prevalence of Permanent Neonatal Diabetes in Slovakia and Successful Replacement of Insulin with Sulfonylurea Therapy in KCNJ11 and ABCC8 Mutation Carriers

CONTEXT: Mutations in the KCNJ11 and ABCC8 genes encoding the pancreatic β-cell K(ATP) channel have recently been shown to be the most common cause of permanent neonatal diabetes mellitus (PNDM). Information regarding the frequency of PNDM has been based mainly on nonpopulation or short-term collect...

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Bibliografiset tiedot
Julkaisussa:J Clin Endocrinol Metab
Päätekijät: Stanik, Juraj, Gasperikova, Daniela, Paskova, Magdalena, Barak, Lubomir, Javorkova, Jana, Jancova, Emilia, Ciljakova, Miriam, Hlava, Peter, Michalek, Jozef, Flanagan, Sarah E., Pearson, Ewan, Hattersley, Andrew T., Ellard, Sian, Klimes, Iwar
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2007
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7611849/
https://ncbi.nlm.nih.gov/pubmed/17213273
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2006-2490
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